Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.47416842C>T , CM000663.2:g.47416842C>T | GRCh38 |
| NC_000001.10:g.47882514C>T , CM000663.1:g.47882514C>T | GRCh37 |
| NC_000001.9:g.47655101C>T | NCBI36 |
| NG_016192.1:g.5771C>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_012186.3:c.527C>T (FOXE3) MANE Select | NP_036318.1:p.Ala176Val |
| ENST00000335071.4:c.527C>T (FOXE3) MANE Select | ENSP00000334472.2:p.Ala176Val |
| NM_012186.2:c.527C>T (FOXE3) | NP_036318.1:p.Ala176Val |
| NR_126355.1:n.29-6941G>A (LINC01389) | |
| ENST00000335071.3:c.527C>T (FOXE3) | ENSP00000334472.2:p.Ala176Val |